Glémain 2002.
Study characteristics | |
Methods |
Study design: parallel‐group randomized trial Study dates: not available Setting: outpatient, multicenter and national Country: France |
Participants |
Inclusion criteria:
Exclusion criteria:
Sample size: 329 randomized participants Age (years): Group 1 mean (SD): 64.4 (7.7) Group 2 mean (SD): 65.2 (7.9) IPSS score (baseline): Group 1 mean (SD): 16.3 (5.6) Group 2 mean (SD): 16.2 (5.2) Prostate size: Group 1 mean (SD): 38.6 (15) Group 2 mean (SD): 40.8 (16.5) |
Interventions |
Group 1 (n = 161): placebo orally after breakfast and dinner for 52 weeks Group 2 (n = 165): Serenoa repens 160 mg orally (Permixon) after breakfast and dinner for 52 weeks Co‐interventions: tamsulosin (Omix LP 0.4 mg) orally after breakfast |
Outcomes |
Urinary symptoms
Quality of life
Adverse events
Other outcomes measured in the trial: sexual function was assessed using the Brief Male Sexual Function Inventory (BMSFI), Qmax |
Notes |
Funding sources: not available Declarations of interest: not available |